核磁共振波谱在先天性代谢缺陷研究中的应用 - Suppr

Suppr

超能文献

Nuclear magnetic resonance spectroscopy in the study of inborn errors of metabolism.

作者信息

Iles R A, Chalmers R A

机构信息

Medical Unit (Section of Metabolism and Endocrinology), London Hospital Medical College, U.K.

出版信息

Clin Sci (Lond). 1988 Jan;74(1):1-10. doi: 10.1042/cs0740001.

DOI:10.1042/cs0740001

PMID:3276437

Abstract

摘要

相似文献

Nuclear magnetic resonance spectroscopy in the study of inborn errors of metabolism.核磁共振波谱在先天性代谢缺陷研究中的应用

Clin Sci (Lond). 1988 Jan;74(1):1-10. doi: 10.1042/cs0740001.

Expanding the diagnostic and research toolbox for inborn errors of metabolism: the role of magnetic resonance spectroscopy.拓展先天性代谢缺陷的诊断和研究工具：磁共振波谱的作用

Mol Genet Metab. 2005 Sep-Oct;86(1-2):2-9. doi: 10.1016/j.ymgme.2005.07.009.

Proton nuclear magnetic resonance urinalysis: coming of age.质子核磁共振尿液分析：走向成熟。

Kidney Int Suppl. 1994 Nov;47:S122-8.

Metabolic studies using 13C nuclear magnetic resonance spectroscopy.

Essays Biochem. 1991;26:105-19.

N-acetylated metabolites in urine: proton nuclear magnetic resonance spectroscopic study on patients with inborn errors of metabolism.尿液中的N-乙酰化代谢物：对先天性代谢缺陷患者的质子核磁共振波谱研究

Clin Chem. 2004 Jan;50(1):58-66. doi: 10.1373/clinchem.2003.020214. Epub 2003 Nov 18.

Nuclear magnetic resonance spectroscopy and genetic disorders.核磁共振波谱学与遗传性疾病

Curr Med Chem. 2008;15(1):15-36. doi: 10.2174/092986708783330719.

Screening for inborn metabolic disorders by 1H-NMR spectrometry.通过¹H-NMR光谱法筛查先天性代谢紊乱。

J Pediatr. 1986 Jan;108(1):166-8. doi: 10.1016/s0022-3476(86)80819-8.

Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometry.使用高分辨率¹H-FT-NMR光谱法对先天性代谢缺陷进行选择性筛查的可能性。

Eur J Pediatr. 1986 Sep;145(4):260-6. doi: 10.1007/BF00439397.

Proton MR spectroscopy of pediatric brain metabolic disorders.小儿脑代谢紊乱的质子磁共振波谱分析

Neuroimaging Clin N Am. 1998 Nov;8(4):781-807.

New frontiers in neuroimaging applications to inborn errors of metabolism.神经影像学在先天性代谢错误中的新应用。

Mol Genet Metab. 2011 Nov;104(3):195-205. doi: 10.1016/j.ymgme.2011.06.020. Epub 2011 Jun 30.

引用本文的文献

Intra- and extracellular carbohydrates in plant cell cultures investigated by (1)H-NMR.（1）H-NMR 研究植物细胞培养物中的细胞内和细胞外碳水化合物。

Plant Cell Rep. 1991 Jan;9(9):527-30. doi: 10.1007/BF00232112.

Diet treatment of branched chain ketoaciduria studied by proton magnetic resonance spectroscopy.质子磁共振波谱研究支链酮酸尿症的饮食治疗。

Amino Acids. 1996 Mar;11(1):91-7. doi: 10.1007/BF00805724.

Diagnosis and follow-up of inborn errors of amino acid metabolism: Use of proton magnetic resonance of biological fluids.氨基酸代谢先天性错误的诊断和随访：生物液的质子磁共振的应用。

Amino Acids. 1996 Dec;10(4):305-15. doi: 10.1007/BF00805859.

Advances in NMR-based biofluid analysis and metabolite profiling.基于 NMR 的生物流体分析和代谢物分析的进展。

Analyst. 2010 Jul;135(7):1490-8. doi: 10.1039/c000091d. Epub 2010 Apr 9.

1H NMR spectroscopy of body fluids in patients with inborn errors of purine and pyrimidine metabolism.嘌呤和嘧啶代谢先天性缺陷患者体液的1H核磁共振波谱分析。

J Inherit Metab Dis. 1997 Jul;20(3):345-50. doi: 10.1023/a:1005313524869.

The role of magnetic resonance spectroscopy in the investigation of lactic acidosis and inborn errors of energy metabolism.磁共振波谱在乳酸酸中毒及先天性能量代谢障碍研究中的作用。

J Inherit Metab Dis. 1996;19(4):548-52. doi: 10.1007/BF01799115.

Analysis of fetal and neonatal urine using proton nuclear magnetic resonance spectroscopy.使用质子核磁共振波谱法分析胎儿和新生儿尿液。

Arch Dis Child Fetal Neonatal Ed. 1995 Nov;73(3):F153-7. doi: 10.1136/fn.73.3.f153.

High-resolution proton nuclear magnetic resonance studies of urine from asphyxiated newborn infants.窒息新生儿尿液的高分辨率质子核磁共振研究。

Appl Biochem Biotechnol. 1995 Apr;53(1):37-51. doi: 10.1007/BF02783480.

Sclerosing cholangitis with hepatic microvesicular steatosis in cystic fibrosis and chronic pancreatitis.囊性纤维化和慢性胰腺炎合并硬化性胆管炎伴肝脏微泡性脂肪变性

J Clin Pathol. 1989 May;42(5):466-9. doi: 10.1136/jcp.42.5.466.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验